Canonical Allele Identifier: CA2577209090
Gene: NDUFB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201078874C>A , CM000664.2:g.201078874C>A GRCh38
NC_000002.11:g.201943597C>A , CM000664.1:g.201943597C>A GRCh37
NC_000002.10:g.201651842C>A NCBI36
NG_032156.1:g.12136C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000450023.6:c.-2-7C>A ENSP00000401834.2:n.-2-7C>A
ENST00000682325.1:c.-2-7C>A ENSP00000507925.1:n.-2-7C>A
ENST00000684175.1:c.-2-7C>A ENSP00000508132.1:n.-2-7C>A
ENST00000684420.1:c.-2-7C>A ENSP00000508208.1:n.-2-7C>A
ENST00000237889.9:c.-2-7C>A MANE Select ENSP00000237889.4:n.-2-7C>A
ENST00000237889.8:c.-2-7C>A ENSP00000237889.4:n.-2-7C>A
ENST00000433898.5:c.-2-7C>A ENSP00000410600.1:n.-2-7C>A
ENST00000450023.5:c.-2-7C>A ENSP00000401834.1:n.-2-7C>A
ENST00000454214.1:c.-2-7C>A ENSP00000407336.1:n.-2-7C>A
NM_001257102.1:c.-2-7C>A NP_001244031.1:n.-2-7C>A
NM_002491.2:c.-2-7C>A NP_002482.1:n.-2-7C>A
XM_011511230.1:c.-2-7C>A XP_011509532.1:n.-2-7C>A
XM_011511230.3:c.-2-7C>A XP_011509532.1:n.-2-7C>A
XM_017004186.2:c.-2-7C>A XP_016859675.1:n.-2-7C>A
NM_002491.3:c.-2-7C>A MANE Select NP_002482.1:n.-2-7C>A
NM_001257102.2:c.-2-7C>A NP_001244031.1:n.-2-7C>A